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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638376Generated: October 25, 2026

Potassium Carbonate → 1-(5-Isoquinolinesulfonyl)-4-isobutylpiperazine

https://huagongshe.com/reaction/638376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-Methylpropyl)piperazineHCID 2052052—
Reactant5-Isoquinolinesulfonyl chlorideHCID 3371655—
ReactantChloroform methanolHCID 21584188—
SolventChloroformHCID 6212—
Product1-(5-Isoquinolinesulfonyl)-4-isobutylpiperazineHCID 1311694078.1%

Reaction Steps

In 30 ml of chloroform were added 1.42 g of 1-isobutylpiperazine and 2.76 g of potassium carbonate, and to the mixture was added dropwise 50 ml of a chloroform solution containing 2.28 g of 5-isoquinolinesulfonyl chloride under cooling with ice. After the dropwise addition of the chloroform solution, the mixed solution thus obtained was stirred at a temperature of 15° C. to 25° C. for two hours, and then the reaction solution was washed with 20 ml of a 1N aqueous sodium hydroxide solution and extracted twice with a 5N aqueous hydrochloric acid solution. The aqueous hydrochloric acid layer was rendered alkaline, extracted three time with 30 ml of chloroform, and the chloroform layer extracted was washed with water and dried with anhydrous magnesium sulfate. After the chloroform was distilled therefrom under reduced pressure, the residue obtained was subjected to a silica gel column chromatography (silica gel: 100 g; solvent: 2% methanol-chloroform) to give 2.60 g of 1-(5-isoquinolinesulfonyl)-4-isobutylpiperazine, i.e., Compound (47) in a yield of 78%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04560755
Source datasetuspto-grants-1985_12
ORD IDord-905fe4a462c74f6d94703c688847030e
Source noteuspto-grants-1985_12